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NCT07339410Completed

Physiotherapy to Improve Balance and Walking Capacity in Hemophilia

Effects of Manual Therapy and Structured Exercises on Postural Balance and Walking Capacity in Adults With Hemophilia

Source: ClinicalTrials.gov · Last updated 14 Jan 2026

Brief summary (registry, in English)

Introduction: Hemarthrosis is the most common type of bleeding with 70-80% in patient with hemophilia (PwH) and the majority of hemarthrosis occurs in the knee and ankle joints. Recurrent hemarthrosis may cause pain, limited range of motion (ROM), atrophy, swelling, crepitus, and decreased proprioceptive sensation and ultimately causes hemophilic arthropathy. Preventing hemarthrosis and treating arthropathy symptoms in PwH may improve static and dynamic balance and walking capacity. The aim of this study was to investigate the effects of manual therapy and structured exercises on joint health, activity pain, walking capacity and static and dynamic balance. Method: Thirty-five AwH were randomly assigned to two groups using the computerised simple randomization method: the control group (CG) and the physiotherapy group (PG). The sample sizes for the CG and PG are 17 and 18, respectively. Hemophilia type and severity, treatment regime (prophylaxis or on-demand), age, height and weight were recorded. Joint health was assessed with Hemophilia Joint Health Score (HJHS) version 2.1 by a hemophilia specialist physiotherapist. Activity pain was assessed with Numeric Pain Scale (NPS). Walking capacity was evaluated 6 Minute Walking Test (6MWT). Postural balance (static and dynamic balance) were evaluated with the Pro-kin Technobody Posturographic Platform (Pro-kin 212, Technobody s.r.l, Dalmine, 21044 Bergamo, Italy). Static stability test was used for static balance assessment. Dynamic balance was evaluated with the Limits of Stability (LoS) test. The PG received 12 physiotherapy sessions twice a week for 6 weeks. The physiotherapy intervention consisted of manual therapy and a structured, progressive exercise program. The CG continued with their routine hemophilia care.

Status (registry)
Completed
Study type
Interventional
Enrollment
35 (actual)
First submitted
5 Jan 2026
Start date
20 Oct 2025
Primary completion date
20 Dec 2025
Lead sponsor
Yuzuncu Yil University
Diseases
Haemophilia
NCT number
NCT07339410

What you commit to

  • Study type: Interventional
  • Participants enrolled: 35
  • From 20 Oct 2025 to the primary completion date, 20 Dec 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Receiving physiotherapy or undergone surgery on lower extremity within the last 6 months

Other illness

  • Having neurological or cognitive disease

Other

  • Having visual and vestibular system pathologies

Who the study is looking for

  • Severe or moderate hemophilia A or B
  • Aged 18-65
  • Having at least 3 points from at least one of the knee and ankle index joints in the Hemophilia Joint Health Score
  • Volunteering to attend physiotherapy sessions regularly

Age in the registry: 18 years to 65 years · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Van Yüzüncü Yıl University
Coordinator of this site? Confirm its status
VanTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.